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Hearing loss

Gene: DVL3

Red List (low evidence)

DVL3 (dishevelled segment polarity protein 3)
EnsemblGeneIds (GRCh38): ENSG00000161202
EnsemblGeneIds (GRCh37): ENSG00000161202
OMIM: 601368, Gene2Phenotype
DVL3 is in 8 panels

2 reviews

Maria Bitner-Glindzicz (UCL)

Red List (low evidence)

Jun Shen (Harvard Medical School)

Red List (low evidence)

DVL3 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:06 a.m.
DVL3 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:41 p.m.

Publications

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

DVL3 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert